功能(生物学)
抗体
效应器
CTLA-4号机组
免疫学
细胞生物学
T细胞
生物
免疫系统
作者
Frederick Arce Vargas,Andrew J.S. Furness,Kevin Litchfield,Kroopa Joshi,Rachel Rosenthal,Ehsan Ghorani,Isabelle Solomon,Marta H. Lesko,Nora Ruef,Claire Roddie,Jake Y. Henry,Lavinia Spain,Assma Ben Aïssa,Andrew Georgiou,Yien Ning Sophia Wong,Myles Smith,D. Strauß,Andrew Hayes,David Nicol,Tim O'Brien
出处
期刊:Cancer Cell
[Elsevier]
日期:2018-03-22
卷期号:33 (4): 649-663.e4
被引量:544
标识
DOI:10.1016/j.ccell.2018.02.010
摘要
With the use of a mouse model expressing human Fc-gamma receptors (FcγRs), we demonstrated that antibodies with isotypes equivalent to ipilimumab and tremelimumab mediate intra-tumoral regulatory T (Treg) cell depletion in vivo, increasing the CD8+ to Treg cell ratio and promoting tumor rejection. Antibodies with improved FcγR binding profiles drove superior anti-tumor responses and survival. In patients with advanced melanoma, response to ipilimumab was associated with the CD16a-V158F high affinity polymorphism. Such activity only appeared relevant in the context of inflamed tumors, explaining the modest response rates observed in the clinical setting. Our data suggest that the activity of anti-CTLA-4 in inflamed tumors may be improved through enhancement of FcγR binding, whereas poorly infiltrated tumors will likely require combination approaches.
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